IL108800A - תולדות 1-מותמרות של 4,5-דיהדרו-]1,2,4[ -טריאזולו]a-3, 4[ קוינוכסאלין -4- און הכנתן ותכשירי רוקחות המכילים אותן - Google Patents
תולדות 1-מותמרות של 4,5-דיהדרו-]1,2,4[ -טריאזולו]a-3, 4[ קוינוכסאלין -4- און הכנתן ותכשירי רוקחות המכילים אותןInfo
- Publication number
- IL108800A IL108800A IL108800A IL10880094A IL108800A IL 108800 A IL108800 A IL 108800A IL 108800 A IL108800 A IL 108800A IL 10880094 A IL10880094 A IL 10880094A IL 108800 A IL108800 A IL 108800A
- Authority
- IL
- Israel
- Prior art keywords
- compound
- triazolo
- quinoxalin
- formula
- trifluoromethyl
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 10
- 238000002360 preparation method Methods 0.000 title description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 141
- 229910052739 hydrogen Inorganic materials 0.000 claims description 48
- -1 Diethoxyphosphoryl Chemical group 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 11
- NPVOJIUIIYMCKF-UHFFFAOYSA-N 5h-[1,2,4]triazolo[4,3-a]quinoxalin-4-one Chemical compound O=C1NC2=CC=CC=C2N2C1=NN=C2 NPVOJIUIIYMCKF-UHFFFAOYSA-N 0.000 claims description 10
- 238000007363 ring formation reaction Methods 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
- 230000002964 excitative effect Effects 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 230000007062 hydrolysis Effects 0.000 claims description 6
- 238000006460 hydrolysis reaction Methods 0.000 claims description 6
- 208000013403 hyperactivity Diseases 0.000 claims description 6
- 125000002883 imidazolyl group Chemical group 0.000 claims description 6
- 230000003042 antagnostic effect Effects 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 239000002858 neurotransmitter agent Substances 0.000 claims description 5
- GUGQQGROXHPINL-UHFFFAOYSA-N 2-oxobutanoyl chloride Chemical compound CCC(=O)C(Cl)=O GUGQQGROXHPINL-UHFFFAOYSA-N 0.000 claims description 4
- 201000006474 Brain Ischemia Diseases 0.000 claims description 4
- 150000001263 acyl chlorides Chemical class 0.000 claims description 4
- 238000006392 deoxygenation reaction Methods 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 230000002140 halogenating effect Effects 0.000 claims description 4
- 238000005984 hydrogenation reaction Methods 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 206010008120 Cerebral ischaemia Diseases 0.000 claims description 3
- 241001465754 Metazoa Species 0.000 claims description 3
- 208000027089 Parkinsonian disease Diseases 0.000 claims description 3
- 206010034010 Parkinsonism Diseases 0.000 claims description 3
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 3
- 206010008118 cerebral infarction Diseases 0.000 claims description 3
- 239000003814 drug Substances 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- WEQYBMHJHXRZKK-UHFFFAOYSA-N (7-cyano-4-oxo-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl)methylphosphonic acid Chemical compound C1=C(C#N)C=C2NC(=O)C3=NN=C(CP(O)(=O)O)N3C2=C1 WEQYBMHJHXRZKK-UHFFFAOYSA-N 0.000 claims description 2
- RYJVPEAORJJXLQ-UHFFFAOYSA-N (7-nitro-4-oxo-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl)methylphosphonic acid Chemical compound C1=C([N+]([O-])=O)C=C2NC(=O)C3=NN=C(CP(O)(=O)O)N3C2=C1 RYJVPEAORJJXLQ-UHFFFAOYSA-N 0.000 claims description 2
- WOALGIJXYCWIGZ-UHFFFAOYSA-N 1-(diethoxyphosphorylmethyl)-7-nitro-5h-[1,2,4]triazolo[4,3-a]quinoxalin-4-one Chemical compound C1=C([N+]([O-])=O)C=C2NC(=O)C3=NN=C(CP(=O)(OCC)OCC)N3C2=C1 WOALGIJXYCWIGZ-UHFFFAOYSA-N 0.000 claims description 2
- KMUOQJDINUXYQG-UHFFFAOYSA-N 1-[4-oxo-7-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl]ethylphosphonic acid Chemical compound C1=C(C(F)(F)F)C=C2NC(=O)C3=NN=C(C(C)P(O)(O)=O)N3C2=C1 KMUOQJDINUXYQG-UHFFFAOYSA-N 0.000 claims description 2
- IMCHMXVRAJDKCC-UHFFFAOYSA-N 3-(7-nitro-4-oxo-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl)propanoic acid Chemical compound C1=C([N+]([O-])=O)C=C2NC(=O)C3=NN=C(CCC(=O)O)N3C2=C1 IMCHMXVRAJDKCC-UHFFFAOYSA-N 0.000 claims description 2
- ZEELIWMJLZIGAH-UHFFFAOYSA-N 3-[4-oxo-7-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl]propanoic acid Chemical compound C1=C(C(F)(F)F)C=C2NC(=O)C3=NN=C(CCC(=O)O)N3C2=C1 ZEELIWMJLZIGAH-UHFFFAOYSA-N 0.000 claims description 2
- NTRWUUMFXLICNH-UHFFFAOYSA-N 3-[7-cyano-4-oxo-8-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl]propanoic acid Chemical compound FC(F)(F)C1=C(C#N)C=C2NC(=O)C3=NN=C(CCC(=O)O)N3C2=C1 NTRWUUMFXLICNH-UHFFFAOYSA-N 0.000 claims description 2
- ZHRYYFRNMKYZIO-UHFFFAOYSA-N 8-amino-1-(diethoxyphosphorylmethyl)-7-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-4-one Chemical compound NC1=C(C(F)(F)F)C=C2NC(=O)C3=NN=C(CP(=O)(OCC)OCC)N3C2=C1 ZHRYYFRNMKYZIO-UHFFFAOYSA-N 0.000 claims description 2
- BYXSOSJQRIWDCH-UHFFFAOYSA-N 8-bromo-1-(1-diethoxyphosphorylethyl)-7-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-4-one Chemical compound BrC1=C(C(F)(F)F)C=C2NC(=O)C3=NN=C(C(C)P(=O)(OCC)OCC)N3C2=C1 BYXSOSJQRIWDCH-UHFFFAOYSA-N 0.000 claims description 2
- 230000002152 alkylating effect Effects 0.000 claims description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N aminomethyl benzene Natural products NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims description 2
- 150000003939 benzylamines Chemical class 0.000 claims description 2
- GQLQDOAJXFSDEP-UHFFFAOYSA-N ethoxy-[[4-oxo-7-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl]methyl]phosphinic acid Chemical compound C1=C(C(F)(F)F)C=C2NC(=O)C3=NN=C(CP(O)(=O)OCC)N3C2=C1 GQLQDOAJXFSDEP-UHFFFAOYSA-N 0.000 claims description 2
- 238000007327 hydrogenolysis reaction Methods 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- CPRRHERYRRXBRZ-SRVKXCTJSA-N methyl n-[(2s)-1-[[(2s)-1-hydroxy-3-[(3s)-2-oxopyrrolidin-3-yl]propan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]carbamate Chemical compound COC(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CO)C[C@@H]1CCNC1=O CPRRHERYRRXBRZ-SRVKXCTJSA-N 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001567 quinoxalinyl group Chemical class N1=C(C=NC2=CC=CC=C12)* 0.000 claims 2
- MGRVRXRGTBOSHW-UHFFFAOYSA-N (aminomethyl)phosphonic acid Chemical compound NCP(O)(O)=O MGRVRXRGTBOSHW-UHFFFAOYSA-N 0.000 claims 1
- USVAIEZCNAPPER-UHFFFAOYSA-N 1-(diethoxyphosphorylmethyl)-4-oxo-5h-[1,2,4]triazolo[4,3-a]quinoxaline-7-carbonitrile Chemical compound C1=C(C#N)C=C2NC(=O)C3=NN=C(CP(=O)(OCC)OCC)N3C2=C1 USVAIEZCNAPPER-UHFFFAOYSA-N 0.000 claims 1
- FQOZQYXJJVQBGI-UHFFFAOYSA-N 1-(diethoxyphosphorylmethyl)-4-oxo-8-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxaline-7-carbonitrile Chemical compound FC(F)(F)C1=C(C#N)C=C2NC(=O)C3=NN=C(CP(=O)(OCC)OCC)N3C2=C1 FQOZQYXJJVQBGI-UHFFFAOYSA-N 0.000 claims 1
- WJDRDHPEAWVUFY-UHFFFAOYSA-N 1-(diethoxyphosphorylmethyl)-8-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-4-one Chemical compound FC(F)(F)C1=CC=C2NC(=O)C3=NN=C(CP(=O)(OCC)OCC)N3C2=C1 WJDRDHPEAWVUFY-UHFFFAOYSA-N 0.000 claims 1
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- MJUJXFBTEFXVKU-UHFFFAOYSA-N diethyl phosphonate Chemical class CCOP(=O)OCC MJUJXFBTEFXVKU-UHFFFAOYSA-N 0.000 description 1
- HSUGRBWQSSZJOP-RTWAWAEBSA-N diltiazem Chemical group C1=CC(OC)=CC=C1[C@H]1[C@@H](OC(C)=O)C(=O)N(CCN(C)C)C2=CC=CC=C2S1 HSUGRBWQSSZJOP-RTWAWAEBSA-N 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- HFWAFHWJTSSWCX-UHFFFAOYSA-N ethyl 3-[4-oxo-7-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl]propanoate Chemical compound C1=C(C(F)(F)F)C=C2NC(=O)C3=NN=C(CCC(=O)OCC)N3C2=C1 HFWAFHWJTSSWCX-UHFFFAOYSA-N 0.000 description 1
- IDZSDQKGWPJLQY-UHFFFAOYSA-N ethyl 3-[7-cyano-4-oxo-8-(trifluoromethyl)-5h-[1,2,4]triazolo[4,3-a]quinoxalin-1-yl]propanoate Chemical compound FC(F)(F)C1=C(C#N)C=C2NC(=O)C3=NN=C(CCC(=O)OCC)N3C2=C1 IDZSDQKGWPJLQY-UHFFFAOYSA-N 0.000 description 1
- GSMBUYNBVVIEDY-UHFFFAOYSA-N ethyl 7-nitro-4-oxo-5h-[1,2,4]triazolo[4,3-a]quinoxaline-1-carboxylate Chemical compound C1=C([N+]([O-])=O)C=C2NC(=O)C3=NN=C(C(=O)OCC)N3C2=C1 GSMBUYNBVVIEDY-UHFFFAOYSA-N 0.000 description 1
- 230000000763 evoking effect Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229940049906 glutamate Drugs 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- GMKMEZVLHJARHF-SYDPRGILSA-N meso-2,6-diaminopimelic acid Chemical compound [O-]C(=O)[C@@H]([NH3+])CCC[C@@H]([NH3+])C([O-])=O GMKMEZVLHJARHF-SYDPRGILSA-N 0.000 description 1
- 239000003158 myorelaxant agent Substances 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 230000004770 neurodegeneration Effects 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 230000016273 neuron death Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 239000002287 radioligand Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000010410 reperfusion Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000003345 scintillation counting Methods 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical compound [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 1
- 229910000367 silver sulfate Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 230000009870 specific binding Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000005062 synaptic transmission Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 210000004127 vitreous body Anatomy 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK93310A DK31093D0 (he) | 1993-03-19 | 1993-03-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL108800A0 IL108800A0 (en) | 1994-06-24 |
| IL108800A true IL108800A (he) | 1998-02-22 |
Family
ID=8092112
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL108800A IL108800A (he) | 1993-03-19 | 1994-03-01 | תולדות 1-מותמרות של 4,5-דיהדרו-]1,2,4[ -טריאזולו]a-3, 4[ קוינוכסאלין -4- און הכנתן ותכשירי רוקחות המכילים אותן |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5559106A (he) |
| EP (1) | EP0691969A1 (he) |
| JP (1) | JPH08507536A (he) |
| KR (1) | KR100313051B1 (he) |
| CN (1) | CN1041930C (he) |
| AU (1) | AU685783B2 (he) |
| CA (1) | CA2158545A1 (he) |
| DK (1) | DK31093D0 (he) |
| FI (1) | FI954386A0 (he) |
| HU (1) | HUT73419A (he) |
| IL (1) | IL108800A (he) |
| NO (1) | NO305286B1 (he) |
| NZ (1) | NZ262365A (he) |
| TW (1) | TW304195B (he) |
| WO (1) | WO1994021639A1 (he) |
| ZA (1) | ZA941926B (he) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4314592A1 (de) * | 1993-04-28 | 1994-11-03 | Schering Ag | Benzo(f)chinoxalindionderivate, deren Herstellung und Verwendung in Arzneimitteln |
| ATE190616T1 (de) * | 1994-09-16 | 2000-04-15 | Novo Nordisk As | (1,2,4)triazolo(4,3-a)chinoxylinonderivate, ihre darstellung und verwendung als antagonisten von ampa-rezeptoren |
| JPH10506620A (ja) * | 1994-09-16 | 1998-06-30 | ノボ ノルディスク アクティーゼルスカブ | 〔１，２，４〕トリアゾロ〔４，３−ａ〕キノキサリノン誘導体、それらの調製方法及び使用 |
| US5679680A (en) * | 1995-02-16 | 1997-10-21 | Warner-Lambert Company | α-substituted hydrazides having calpain inhibitory activity |
| FR2743363A1 (fr) * | 1996-01-10 | 1997-07-11 | Rhone Poulenc Rorer Sa | 5h,10h-imidazo(1,2-a)indeno(1,2-e)pyrazine-a-ones substituees en position 2, leur preparation et les medicaments les contenant |
| IL125950A0 (en) * | 1997-09-05 | 1999-04-11 | Pfizer Prod Inc | Methods of administering ampa receptor antagonists to treat dyskinesias associated with dopamine agonist therapy |
| WO1999024434A1 (en) | 1997-11-11 | 1999-05-20 | Ono Pharmaceutical Co., Ltd. | Fused pyrazine compounds |
| AU2298399A (en) * | 1998-02-06 | 1999-08-23 | Yoshitomi Pharmaceutical Industries, Ltd. | Novel azapeptide type hydroxamic acid derivatives |
| US20040152694A1 (en) * | 2003-02-04 | 2004-08-05 | Istvan Kurucz | Methods and compositions for treating inflammatory disorders of the airways |
| WO2008072779A1 (ja) * | 2006-12-13 | 2008-06-19 | Aska Pharmaceutical Co., Ltd. | キノキサリン誘導体 |
| AU2010219598A1 (en) | 2009-03-05 | 2011-09-22 | Astellas Pharma Inc. | Quinoxaline compounds |
| EP2338492A1 (en) | 2009-12-24 | 2011-06-29 | Universidad del Pais Vasco | Methods and compositions for the treatment of alzheimer |
| CA2810659A1 (en) | 2010-09-07 | 2012-03-15 | Astellas Pharma Inc. | Quinoxaline compound |
| EP2723744B1 (en) * | 2011-06-27 | 2016-03-23 | Janssen Pharmaceutica, N.V. | 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES |
| ES2855575T3 (es) | 2012-06-26 | 2021-09-23 | Janssen Pharmaceutica Nv | Combinaciones que comprenden compuestos de 4-metil-[1,2,4]triazolo[4,3-a]quinoxalina como inhibidores de PDE2 e inhibidores de PDE10 para su uso en el tratamiento de trastornos neurológicos o metabólicos |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4354027A (en) * | 1980-05-19 | 1982-10-12 | Usv Pharmaceutical Corporation | Triazoloquinoxalin-4-ones |
| US4547501A (en) * | 1983-09-02 | 1985-10-15 | Pfizer Inc. | Method of using [1,2,4]triazolo[4,3-a]quinoxaline-4-amine derivatives as antidepressant and antifatigue agents |
| US5153196A (en) * | 1991-06-05 | 1992-10-06 | Eli Lilly And Company | Excitatory amino acid receptor antagonists and methods for the use thereof |
| AU3767793A (en) * | 1992-04-03 | 1993-11-08 | Yamanouchi Pharmaceutical Co., Ltd. | Fused quinoxalinone derivative and pharmaceutical composition containing the same |
-
1993
- 1993-03-19 DK DK93310A patent/DK31093D0/da not_active Application Discontinuation
-
1994
- 1994-02-25 CA CA002158545A patent/CA2158545A1/en not_active Abandoned
- 1994-02-25 NZ NZ262365A patent/NZ262365A/en unknown
- 1994-02-25 HU HU9502726A patent/HUT73419A/hu unknown
- 1994-02-25 JP JP6520538A patent/JPH08507536A/ja active Pending
- 1994-02-25 AU AU62018/94A patent/AU685783B2/en not_active Ceased
- 1994-02-25 CN CN94191979A patent/CN1041930C/zh not_active Expired - Fee Related
- 1994-02-25 KR KR1019950703970A patent/KR100313051B1/ko not_active IP Right Cessation
- 1994-02-25 EP EP94908979A patent/EP0691969A1/en not_active Withdrawn
- 1994-02-25 WO PCT/DK1994/000077 patent/WO1994021639A1/en not_active Application Discontinuation
- 1994-02-28 TW TW083101703A patent/TW304195B/zh active
- 1994-03-01 IL IL108800A patent/IL108800A/he active IP Right Grant
- 1994-03-18 ZA ZA941926A patent/ZA941926B/xx unknown
- 1994-12-07 US US08/350,744 patent/US5559106A/en not_active Expired - Fee Related
-
1995
- 1995-09-18 NO NO953673A patent/NO305286B1/no not_active IP Right Cessation
- 1995-09-18 FI FI954386A patent/FI954386A0/fi unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR100313051B1 (ko) | 2002-02-28 |
| HU9502726D0 (en) | 1995-11-28 |
| IL108800A0 (en) | 1994-06-24 |
| AU685783B2 (en) | 1998-01-29 |
| EP0691969A1 (en) | 1996-01-17 |
| US5559106A (en) | 1996-09-24 |
| CN1041930C (zh) | 1999-02-03 |
| DK31093D0 (he) | 1993-03-19 |
| ZA941926B (en) | 1995-09-18 |
| TW304195B (he) | 1997-05-01 |
| NO953673D0 (no) | 1995-09-18 |
| WO1994021639A1 (en) | 1994-09-29 |
| CN1122601A (zh) | 1996-05-15 |
| NO305286B1 (no) | 1999-05-03 |
| HUT73419A (en) | 1996-07-29 |
| JPH08507536A (ja) | 1996-08-13 |
| FI954386A (fi) | 1995-09-18 |
| FI954386A0 (fi) | 1995-09-18 |
| NZ262365A (en) | 1997-05-26 |
| NO953673L (no) | 1995-11-17 |
| KR960701057A (ko) | 1996-02-24 |
| CA2158545A1 (en) | 1994-09-29 |
| AU6201894A (en) | 1994-10-11 |
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| EP0698024B1 (en) | [1,2,4]TRIAZOLO [4,3-a]QUINOXALINE COMPOUNDS, THEIR PREPARATION AND USE | |
| EP0743945B1 (en) | Heterocyclic compounds and their preparation and use | |
| US6001832A (en) | [1,2,4]triazolo[4,3-a]quinoxalinone derivatives, their preparation and use | |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| KB | Patent renewed |